Evidence map›Paper›PMID 30277102›Full record

Trial reportLeukemia & lymphoma2019

Obinutuzumab plus CHOP is effective and has a tolerable safety profile in previously untreated, advanced diffuse large B-cell lymphoma: the phase II GATHER study.

Jeff P Sharman, Andres Forero-Torres, Luciano J Costa, Ian W Flinn, Lowell Inhorn, Kevin Kelly, Alberto Bessudo, Luis E Fayad, Mark S Kaminski, Andrew M Evens and 8 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Leukemia & lymphoma, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Trial
  2. Trial
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  4. Article
  5. [Chinese expert consensus on short duration infusion of obinutuzumab (2024)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Jeff P Sharmana Willamette Valley Cancer Institute and Research Center , US Oncology Research , Eugene , OR , USA.
Andres Forero-Torresb University of Alabama School of Medicine , Birmingham , AL , USA.
Luciano J Costac Division of Hematology/Oncology , Medical University of South Carolina , Charleston , SC , USA.
Ian W Flinnd Sarah Cannon Research Institute , Nashville , TN , USA.
Lowell Inhorne Blue Ridge Cancer Care , Roanoke , VA , USA.
Kevin Kellyf USC Norris Comprehensive Cancer Center , Los Angeles , CA , USA.
Alberto Bessudog California Cancer Associates for Research and Excellence , San Diego , CA , USA.
Luis E Fayadh Department of Lymphoma and Myeloma , M.D. Anderson Cancer Center, University of Texas , Houston , TX , USA.
Mark S Kaminskii Division of Hematology/Oncology , University of Michigan Comprehensive Cancer Center, Ann Arbor , MI , USA.
Andrew M Evensj Rutgers Cancer Institute of New Jersey , New Brunswick , NJ , USA.
Christopher R Flowersk Winship Cancer Institute , Atlanta , GA , USA.
Deniz Sahinl F. Hoffmann-La Roche Ltd , Basel , Switzerland.
Kirsten E Mundtl F. Hoffmann-La Roche Ltd , Basel , Switzerland.
Thomas Sandmannm Genentech Inc. , South San Francisco , CA , USA.
Günter Fingerle-Rowsonl F. Hoffmann-La Roche Ltd , Basel , Switzerland.
Charlotte Vignall F. Hoffmann-La Roche Ltd , Basel , Switzerland.
Mehrdad Mobasherm Genentech Inc. , South San Francisco , CA , USA.
Andrew D Zelenetzn Memorial Sloan Kettering Cancer Center and Weill Cornell Medical Center , New York , NY , USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

This study investigated the safety and efficacy of obinutuzumab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (G-CHOP) in patients with advanced diffuse large B-cell lymphoma (DLBCL) and explored the impact of cell-of-origin (COO) on patient outcomes. Patients (N = 100) received obinutuzumab (1000 mg on the days 1, 8, and 15 of cycle 1, and day 1 of cycles 2-8) plus CHOP (cycles 1-6). For patients without grade ≥3 infusion-related reactions (IRRs) to standard-rate obinutuzumab infusion, a shorter duration of infusion (SDI) was evaluated. Overall and complete response rates, as determined according to the Cheson et al. criteria by investigators/independent radiological facility, were 82.0/75.0% and 55.0/58.0%, respectively. SDI of 120 minutes and 90 minutes were well tolerated with no grade ≥3 IRRs. Among all patients, IRRs typically occurred during cycle 1, day 1. G-CHOP is active and has an acceptable safety profile in the first-line treatment of patients with advanced DLBCL. Clinical Trials: NCT01414855DLBCL.

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCyclophosphamideDoxorubicinDrug InteractionsDrug MonitoringFemaleHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedNeoplasm StagingPrednisoneAntibodies, Monoclonal, HumanizedCyclophosphamideDoxorubicinobinutuzumabPrednisoneVincristineEfficacyobinutuzumabsafety profile

Identifiers

PMID30277102
PMCPMC6445782

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.